Thiophene, 4-ethyl-2-methyl- is a heterocyclic organic compound characterized by a five-membered ring containing four carbon atoms and one sulfur atom. This compound features ethyl and methyl substituents at the 4 and 2 positions, respectively, which influence its chemical properties and reactivity. It is a colorless to pale yellow liquid with a distinctive odor, often associated with sulfur-containing compounds. The presence of the sulfur atom in the thiophene ring contributes to its aromaticity, making it relatively stable and less reactive than non-aromatic compounds. Thiophene derivatives, including this compound, are known for their applications in organic electronics, pharmaceuticals, and as intermediates in chemical synthesis. The compound's solubility in organic solvents and its moderate volatility are important characteristics for its use in various industrial applications. Additionally, its structure allows for potential participation in electrophilic substitution reactions, making it a versatile building block in organic chemistry. Safety data should be consulted for handling and exposure guidelines, as with all chemical substances.

Thiophene, 4-ethyl-2-methyl-

13678-54-1: Thiophene, 4-ethyl-2-methyl- is a heterocyclic organic compound characterized by a five-membered ring containing four carbon atoms and one sulfur atom. This compound features ethyl and methyl substituents at the 4 and 2 positions, respectively, which influence its chemical properties and reactivity. It is a colorless to pale yellow liquid with a distinctive odor, often associated with sulfur-containing compounds. The presence of the sulfur atom in the thiophene ring contributes to its aromaticity, making it relatively stable and less reactive than non-aromatic compounds. Thiophene derivatives, including this compound, are known for their applications in organic electronics, pharmaceuticals, and as intermediates in chemical synthesis. The compound's solubility in organic solvents and its moderate volatility are important characteristics for its use in various industrial applications. Additionally, its structure allows for potential participation in electrophilic substitution reactions, making it a versatile building block in organic chemistry. Safety data should be consulted for handling and exposure guidelines, as with all chemical substances.

CAS 13678-54-1

Thiophene, 4-ethyl-2-methyl-

4-Ethyl-2-methylthiophene

Ref: IN-DA0012D1

4-Ethyl-2-methylthiophene

Ref: 3D-NAA67854